20735-33-5

Basic information

• Product Name: 2-Aminocyclopentene-1-carbodithioic acid
• Synonyms: 2-Amino-1-cyclopentene-1-carbodithioic acid;2-Aminocyclopentene-1-carbodithioic acid
• CAS NO: 20735-33-5
• Molecular Formula: C₆H₉NS₂
• Molecular Weight: 159.27
• Mol File: 20735-33-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 243.5°C at 760 mmHg
• Flash Point: 101.1°C
• Appearance: /
• Density: 1.303g/cm³
• Vapor Pressure: 0.032mmHg at 25°C
• Refractive Index: 1.675
• CAS DataBase Reference: 2-Aminocyclopentene-1-carbodithioic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Aminocyclopentene-1-carbodithioic acid(20735-33-5)
• EPA Substance Registry System: 2-Aminocyclopentene-1-carbodithioic acid(20735-33-5)

Safety Data

• Hazardous Substances Data: 20735-33-5(Hazardous Substances Data)

Usage

Chemical compound

2-Aminocyclopentene-1-carbodithioic acid

InChI:InChI=1/C6H9NS2/c7-5-3-1-2-4(5)6(8)9/h1-3,7H2,(H,8,9)

Upstream product

• 120-92-3 cyclopentanone 
• 75-15-0 carbon disulfide 

Downstream Products

• 132609-07-5 diphenylantimony(III)-2-aminocyclopentene-1-carbodithioate 
• 186131-76-0 [Ru(C₆H₈NS₂)2(P(C₆H₅)3)2] 
• 91732-60-4 methyl 2-{N-[2-(2'-hydroxyphenyl)methylidenenitrilo]ethyl}amino-1-cyclopentene-dithiocarboxylate 
• 886579-04-0 Bz₂SnCl(2-amino-1-cyclopentene-1-carbodithioic acid^(1-)) 
• 356797-61-0 [Ph₃Sn(2-amino-1-cyclopentene-1-carbodithioate)] 
• 356797-59-6 [Ph₂SnCl(2-amino-1-cyclopentene-1-carbodithioate)] 
• 440642-66-0 2-N-benzylamino-1-cyclopentene-1-carbodithioic acid 
• 67375-00-2 (R,R)-N,N'-bis[α-methylbenzyl]thiourea 
• 56424-41-0 (R)-N-cyclopentylidene-N-(1-phenylethyl)amine 
• 67683-62-9 2-N-cyclohexylaminocyclopent-1-ene-1-carbodithioic acid 

Relevant articles and documents

Synthesis, characterization and bioevaluation of (Z)-4-substituted phenyl- 2-((2-oxoindolin-3-ylidene)aminocyclopent-1-ene carbodithioate) derivatives from 2-aminocyclopent-1-ene carbodithioic acid

A series of oxoindoline derivatives 6(a-e) have been synthesized. Treatment of cyclopentanone (1) with carbon disulphide (2) in liq. NH3 yielded 2-amino-cyclopent-1-enecarbodithioic acid (3) which on further treatment with isatin (4) in ethanol